Research into the role of neurotransmitter systems in the reinforcing effects of cocaine has traditionally focused on monoamines;however recent studies in rodents indicate a strong involvement of glutamatergic mechanisms, particularly during abstinence. Glutamate is an important transmitter due to its prominent role in synaptic plasticity and the remodeling of synapses. We have previously demonstrated significant alterations within the dopamine system of nonhuman primates following chronic cocaine self-administration and abstinence. Given the close reciprocal association between the dopamine and glutamate systems, we hypothesize, therefore, that the glutamate system in these monkeys is also significantly dysregulated. These hypotheses are supported by evidence from animal studies demonstrating direct effects of chronic cocaine exposure and abstinence on the glutamate system. We propose to test these hypotheses by measuring the concentrations of metabotropic glutamate receptors in monkeys previously studied. Thus, one of the significant advantages of the present application is our ability to relate any changes observed in the glutamate system back to previous findings of neurochemical dysregulation in the same animals. The dopamine and glutamate systems have been shown to be closely related to each other in terms of reciprocal regulation. Changes in one system can have significant consequences for regulation of the other. This application will test the hypotheses that elements of the glutamate system is altered in nonhuman primates self-administering cocaine, followed by abstinence, in which the dopamine system has already been extensively characterized, and shown to be substantially dysregulated.

Public Health Relevance

The dopamine and glutamate systems have been shown to be closely related to each other in terms of reciprocal regulation. Changes in one system can have significant consequences for regulation of the other. This application will test the hypotheses that elements of the glutamate system is altered in nonhuman primates self-administering cocaine, followed by abstinence, in which the dopamine system has already been extensively characterized, and shown to be substantially dysregulated.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Small Research Grants (R03)
Project #
1R03DA026590-01A1
Application #
7739660
Study Section
Neurobiology of Motivated Behavior Study Section (NMB)
Program Officer
Frankenheim, Jerry
Project Start
2009-06-15
Project End
2011-05-31
Budget Start
2009-06-15
Budget End
2010-05-31
Support Year
1
Fiscal Year
2009
Total Cost
$71,623
Indirect Cost
Name
Wake Forest University Health Sciences
Department
Physiology
Type
Schools of Medicine
DUNS #
937727907
City
Winston-Salem
State
NC
Country
United States
Zip Code
27157
Crawford, Jordan T; Roberts, David C S; Beveridge, Thomas J R (2013) The group II metabotropic glutamate receptor agonist, LY379268, decreases methamphetamine self-administration in rats. Drug Alcohol Depend 132:414-9
Beveridge, T J R; Smith, H R; Nader, M A et al. (2011) Group II metabotropic glutamate receptors in the striatum of non-human primates: dysregulation following chronic cocaine self-administration. Neurosci Lett 496:15-9